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Lauramide DEA

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Identification
Molecular formula
C14H29NO2
CAS number
120-40-1
IUPAC name
N-(2-hydroxyethyl)dodecanamide
State
State
At room temperature, Lauramide DEA is generally a solid, although it can be found in liquid form as a mixture with other substances or at elevated temperatures.
Melting point (Celsius)
56.00
Melting point (Kelvin)
329.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
257.39g/mol
Molar mass
257.4330g/mol
Density
0.9800g/cm3
Appearence

Lauramide DEA typically appears as a solid that can vary from white to a pale yellow color. It may also be available in liquid form at certain temperatures. The compound's solid form is usually granular or flaky.

Comment on solubility

Solubility of N-(2-hydroxyethyl)dodecanamide

N-(2-hydroxyethyl)dodecanamide, with the chemical formula C14H29NO2, exhibits interesting solubility characteristics due to its unique structure. This compound is an amide derived from dodecanoic acid and is characterized by a long hydrophobic hydrocarbon chain and a polar hydroxyl group. Here are some key points regarding its solubility:

  • Solvent compatibility: N-(2-hydroxyethyl)dodecanamide is generally more soluble in organic solvents such as ethanol, acetone, and chloroform due to its non-polar hydrocarbon tail.
  • Polar interactions: The presence of the hydroxyl group allows for potential hydrogen bonding, enhancing solubility in polar solvents.
  • Water solubility: While it has some solubility in water, it is considered to be moderately soluble due to the opposing characteristics of its hydrophobic and hydrophilic components.
  • Concentration dependence: The solubility may increase at elevated temperatures, making it more viable in formulations requiring higher concentrations.

As with many amides, the balance between hydrophilic and hydrophobic regions plays a crucial role in its overall solubility profile. This dual nature not only influences its solubility but also its applications in various chemical and industrial environments.

Interesting facts

Exploring N-(2-hydroxyethyl)dodecanamide

N-(2-hydroxyethyl)dodecanamide is a fascinating compound with a variety of applications in the realms of chemistry and material science. This compound belongs to the family of fatty acid amides, which are often recognized for their surfactant properties and biological significance.

Key Facts:

  • Biocompatibility: Due to its structure, N-(2-hydroxyethyl)dodecanamide exhibits excellent biocompatibility, making it a valuable candidate for pharmaceutical and biomedical applications.
  • Surfactant Properties: This compound can act as a surfactant, aiding in emulsification and dispersion processes. It is often investigated for its potential use in formulations where modification of surface properties is desired.
  • Environmental Impact: The molecule's fatty-acid component indicates that it may be biodegradable, which is an essential factor in today’s chemistry, focusing on sustainable and eco-friendly materials.
  • Chemical Versatility: N-(2-hydroxyethyl)dodecanamide can undergo various chemical reactions, allowing it to be modified into numerous derivatives that can enhance its properties for specific applications.

In the world of chemical research, compounds like N-(2-hydroxyethyl)dodecanamide are not just interesting for their theoretical properties, but also for their potential practical benefits. As one researcher stated, “The exploration of fatty acid derivatives opens new avenues for innovation in green chemistry.”

This compound’s unique structure, with its hydroxyethyl group, grants it specific functionalities that can be tailored for applications ranging from cosmetics to advanced materials. As studies continue to emerge, the full potential of N-(2-hydroxyethyl)dodecanamide remains an exciting area of exploration.

Synonyms
N-(2-HYDROXYETHYL)DODECANAMIDE
142-78-9
Lauric acid monoethanolamide
Lauramide MEA
N-Lauroylethanolamine
Laurylethanolamide
Lauric monoethanolamide
Amisol LDE
Copramyl
Dodecanamide, N-(2-hydroxyethyl)-
Vistalan
N-(2-Hydroxyethyl)lauramide
Ultrapole H
Comperlan LM
Cyclomide LM
Lauridit LM
Lauroyl-EA
Rolamid CM
Stabilor CMH
Crillon LME
Lauric ethylolamide
Lauroyl monoethanolamide
Steinamid L 203
2-Dodecanamidoethanol
Rewomid L 203
Laurylamidoethanol
Amisol LME
Lauric acid ethanolamide
Lauryl ethanolamide
Lauric acid monoethanolamine
Lauric N-(2-hydroxyethyl)amide
Lauroyl-ethanolamine
Monoethanolamine lauric acid amide
CCRIS 4834
HSDB 5644
EINECS 205-560-1
N-(Dodecanoyl)-ethanolamine
Lauryl monoethanolamide
098P2IGT76
MFCD00020561
N-(dodecanoyl)ethanolamine
DTXSID5025493
LAURAMIDE MONOETHANOLAMIDE
N-(2-Hydroxyethyl)dodecaneamide
CHEBI:85263
NAE 12:0
N-(2-HYDROXYETHYL)DODECANAMIDE [HSDB]
Dodecylethanol amide
Coconut monoethanolamide
UNII-098P2IGT76
Incromide LCL
Mackamide LMM
Ablumide LME
Hartamide LMEA
Lauroylethanolamide
2Dodecanamidoethanol
NAE
Stabilor C.M.H.
Crillon L.M.E.
Alkamide L-203
dodecanoyl ethanolamide
1:1 Cocamide MEA
1:1 Lauramide MEA
N-dodecanoylethanolamine
N-LEA
N(2Hydroxyethyl)lauramide
Empilan LME (Salt/Mix)
Lauramide-MEA (1:1)
ALKAMIDE L 203
N(2Hydroxyethyl)dodecanamide
Lauric N(2hydroxyethyl)amide
LAURAMIDE MEA [INCI]
SCHEMBL679082
TOHOL N 120
CHEMBL246914
Dodecanamide, N(2hydroxyethyl)
DTXCID205493
Cocomonoethanolamide (Salt/Mix)
Dodecanamide, N-2-hydroxyethyl-
LMFA08040041
XH0834
AKOS010638882
CS-W022897
DS-2807
lauric acid monoethanolamide, AldrichCPR
N-(BETA-HYDROXYETHYL)DODECANAMIDE
SY110473
NS00005328
EN300-7367571
Q27158443
Z808715244
205-560-1